نتایج جستجو برای: dansyl chloride

تعداد نتایج: 88201  

Journal: :The Journal of clinical investigation 1999
H F Zhang J Yu E Bajwa S L Morrison S Tomlinson

Complement is involved in the pathogenesis of many diseases, and there is great interest in developing inhibitors of complement for therapeutic application. CD59 is a natural membrane-bound inhibitor of the cytolytic complement membrane attack complex (MAC). In this study, the preparation and characterization of antibody-CD59 (IgG-CD59) chimeric fusion proteins are described. Constructs were co...

Journal: :Chemical communications 2010
Lin Chen Steven Revel Kyle Morris Dave J Adams

Energy transfer between a naphthalene-dipeptide and either a hosted dansyl acceptor or a co-assembling anthracene-dipeptide acceptor occurs on formation of a hydrogel by decreasing the pH.

Journal: :Nucleic acids research 1998
H Hakala P Virta H Salo H Lönnberg

Porous, uniformly sized (50 micrometer) glycidyl methacrylate/ethylene dimethacrylate particles (SINTEF) were used as a solid phase to construct a sandwich type hybridization assay that allowed simultaneous detection of up to six oligonucleotides from a single sample. The assay was based on categorization of the particles by two organic prompt fluorophores, viz. fluorescein and dansyl, and quan...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1992
L Lorand P T Velasco S N Murthy J Wilson K N Parameswaran

The transglutaminase (protein-glutamine: amine gamma-glutamyltransferase, EC 2.3.2.13)-catalyzed cross-linking of proteins in biological systems can often be inhibited by inclusion of small primary amines or glutamine-containing peptides, which act as site-specific blockers of the relevant acceptor (i.e., glutamine) and donor (i.e., lysine) functionalities of the natural substrates. Compounds s...

Journal: :Biochemistry 1999
M L Scalley S Nauli S T Gladwin D Baker

We use a broad array of biophysical methods to probe the extent of structure and time scale of structural transitions in the protein L denatured state ensemble. Measurement of amide proton exchange protection during the first several milliseconds following initiation of refolding in 0.4 M sodium sulfate revealed weak protection in the first beta-hairpin and helix. A tryptophan residue was intro...

Journal: :The Journal of biological chemistry 1979
S Friedman

The minor base 3-(3-amino-3-carboxypropyl)uridine (acp3U) in Escherichia coli tRNAPhe was acylated with the N-hydroxysuccinimide esters of acetic, phenoxy-acetic, and naphthoxyacetic acid, as well as the ester of 5-dimethylaminonaphthalene-1-sulfonyl (dansyl)-glycine. The derivatives of tRNAPhe formed were all capable of accepting phenylalanine. There were only minor effects on the kinetic para...

Journal: :FEBS letters 2006
Lopamudra Homchaudhuri Satish Kumar Rajaram Swaminathan

The onset of hen egg white lysozyme aggregation on exposure to alkaline pH of 12.2 and subsequent slow growth of soluble lysozyme aggregates (at 298 K) was directly monitored by steady-state and time-resolved fluorescence anisotropy of covalently attached dansyl probe over a period of 24 h. The rotational correlation time accounting for tumbling of lysozyme in solution (40 microM) increased fro...

Journal: :Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 2005
Takayuki Asami Hisanori Imura Akira Ohashi Kousaburo Ohashi Tetsuya Ishiwata

A novel absolute determination method using chirality without any calibration curves or comparison standards has been proposed for phosphorus-containing amino acid-type herbicides, glufosinate (D,L-GLUF) and bialaphos (BIAL). This method is based on a change in the enantiomeric ratio after the spiking of a known amount of the enantiomers with different enantiomeric ratios to a sample. D,L-GLUF ...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2007
Chandra Prakash John O'Donnell S Cyrus Khojasteh-Bakht

The excretion, biotransformation, and pharmacokinetics of ezlopitant [(2-benzhydryl-1-aza-bicyclo[2.2.2]oct-3-yl)-(5-isopropyl-2-methoxy-benzyl)-amine], a substance P receptor antagonist, were investigated in healthy male volunteers after oral administration of a single 200-mg (approximately 93 microCi/subject) dose of [(14)C]ezlopitant. The total recovery of administered radioactive dose was 8...

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